Allele Registry

Canonical Allele Identifier: PA274777

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000171557

ClinVar Variation:

191374

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Pro286Ser	CA274776 NM_000159.4:c.856C>T