Allele Registry

Canonical Allele Identifier: PA645479895

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000224360

ClinVar Variation:

235858

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Gln144Pro	CA10581470 NM_000159.4:c.431A>C