Allele Registry

Canonical Allele Identifier: PA658676650

Gene: GCDH HGNC NCBI

ClinVar Allele:

468497

ClinVar RCV:

RCV000530261

ClinVar Variation:

459952

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Ser246Leu	CA9234477 NM_000159.4:c.737C>T