PR:000000113	noggin sequence variant W217G (human)	hNOG/var:W217G|noggin sequence variant 6 (human)|UniProtKB:Q13253, Trp-217, CHEBI:29947		associated_with_disease_progression	DOID:0050788	proximal symphalangism			PMID:10080184	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_011363	20080301	PRO:CNA