Allele Registry

Canonical Allele Identifier: PA095242

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000002163

RCV000224804

ClinVar Variation:

2082

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Ala421Val	CA252095 NM_000159.4:c.1262C>T