Allele Registry

Canonical Allele Identifier: PA2825078594

Gene: GCK HGNC NCBI

ClinVar Variation Id: 2664359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Gly444Asp	CA367396980 NM_000162.5:c.1331G>A