Allele Registry

Canonical Allele Identifier: PA220439

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000179724

ClinVar Variation:

92533

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Glu181Gly	CA220438 NM_000159.4:c.542A>G