Allele Registry

Canonical Allele Identifier: PA916008971

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000169574

RCV000255875

ClinVar Variation:

189150

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Arg88Cys	CA274425 NM_013976.3:c.262C>T