Allele Registry

Canonical Allele Identifier: PA095219

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000521789

RCV000674015

RCV003409413

ClinVar Variation:

286241

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Ala382Thr	CA9234619 NM_000159.4:c.1144G>A