Allele Registry

Canonical Allele Identifier: PA2825070029

Gene: GCDH HGNC NCBI

ClinVar Allele:

928855

ClinVar RCV:

RCV001223617

ClinVar Variation:

951653

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg227Gln	CA9234463 NM_000159.4:c.680G>A