Allele Registry

Canonical Allele Identifier: PA645479955

Gene: GCDH HGNC NCBI

ClinVar Allele:

358598

ClinVar RCV:

RCV000411040

RCV001556801

ClinVar Variation:

370244

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Pro248Leu	CA16041971 NM_000159.4:c.743C>T