Allele Registry

Canonical Allele Identifier: PA2830123778

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000440624

RCV003325955

ClinVar Variation:

381598

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Val366Met	CA16605802 NM_033508.3:c.1096G>A