Allele Registry

Canonical Allele Identifier: PA645479964

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000495869

ClinVar Variation:

430833

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg294Pro	CA404319364 NM_000159.4:c.881G>C