Allele Registry

Canonical Allele Identifier: PA095312

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000634885

RCV000735163

ClinVar Variation:

529442

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg257Gln	CA9234482 NM_000159.4:c.770G>A