Allele Registry

Canonical Allele Identifier: PA2830123452

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003330053

ClinVar Variation:

2580858

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Val225Gly	CA367401120 NM_033508.3:c.674T>G