Allele Registry

Canonical Allele Identifier: PA916009174

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000495869

ClinVar Variation:

430833

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Arg294Pro	CA404319364 NM_013976.3:c.881G>C