PR:000000111	noggin sequence variant G189C (human)	hNOG/var:G189C|noggin sequence variant 4 (human)|UniProtKB:Q13253, Gly-189, CHEBI:29950		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:99178269	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011362	20080301	PRO:CNA