Allele Registry

Canonical Allele Identifier: PA916008993

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000665561

ClinVar Variation:

550735

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Gly101Arg	CA404315959 NM_013976.3:c.301G>A CA404315973 NM_013976.3:c.301G>C