Allele Registry

Canonical Allele Identifier: PA645479863

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000284260

RCV000671394

ClinVar Variation:

288248

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Ser119Leu	CA10606016 NM_000159.4:c.356C>T