Allele Registry

Canonical Allele Identifier: PA2827936694

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003060105

ClinVar Variation:

2136520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Gly223Val	CA367401157 NM_001354800.1:c.668G>T