Allele Registry

Canonical Allele Identifier: PA645460718

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000440624

RCV003325955

ClinVar Variation:

381598

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Val368Met	CA16605802 NM_033507.3:c.1102G>A