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Protein Ontology report - noggin sequence variant P223L (human) PR:000000108 - http://purl.obolibrary.org/obo/PR_000000108        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000108      PRO name noggin sequence variant P223L (human)    Synonyms PRO-Short-label: EXACT: hNOG/var:P223L PRO-proteoform-std: EXACT: UniProtKB:Q13253, Pro-223, CHEBI:30006 Other: EXACT: noggin sequence variant 10 (human)   Definition "A noggin (human) that has a Leu residue at the position equivalent to Pro-223 of the amino acid sequence represented by UniProtKB:Q13253. UniProtKB:Q13253, Pro-223, CHEBI:30006." [PMID:10080184, PRO:CNA, PRO:DAN]    PRO Category organism-sequence    Parent PR:Q13253 noggin (human)   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_011367 Back to top Functional Annotation (GO-centric view) Switch to PRO Centric View       Disease Associated GO Term Protein Forms & Complexes Evidence DO:0050788 proximal symphalangism PR:000000108 hNOG/var:P223L PMID:10080184