Allele Registry

Canonical Allele Identifier: PA2830123436

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000502130

RCV000517681

RCV000763585

RCV002367690

RCV003403165

ClinVar Variation:

435306

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Gly222Ser	CA367401165 NM_033508.3:c.664G>A