Allele Registry

Canonical Allele Identifier: PA916039408

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029851

RCV000711759

RCV001248969

RCV003398573

RCV004017269

ClinVar Variation:

36188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Lys92Glu	CA213739 NM_001354803.2:c.274A>G