Allele Registry

Canonical Allele Identifier: PA916039376

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000440624

RCV003325955

ClinVar Variation:

381598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Val45Met	CA16605802 NM_001354803.2:c.133G>A