Allele Registry

Canonical Allele Identifier: PA2830123437

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003325674

ClinVar Variation:

2578075

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Gly222Arg	CA367401164 NM_033508.3:c.664G>C