Allele Registry

Canonical Allele Identifier: PA645479870

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000444441

RCV000553882

ClinVar Variation:

377917

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg132Gln	CA16608038 NM_000159.4:c.395G>A