Allele Registry

Canonical Allele Identifier: PA2830123888

Gene: GCK HGNC NCBI

ClinVar Variation Id: 995101

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Gly387Asp	CA367398670 NM_033508.3:c.1160G>A