Allele Registry

Canonical Allele Identifier: PA2830122233

Gene: GCK HGNC NCBI

ClinVar Variation Id: 995101

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly389Asp	CA367398670 NM_033507.3:c.1166G>A