Allele Registry

Canonical Allele Identifier: PA095517

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000665561

ClinVar Variation:

550735

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Gly101Arg	CA404315959 NM_000159.4:c.301G>A CA404315973 NM_000159.4:c.301G>C