Allele Registry

Canonical Allele Identifier: PA2827936706

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003330054

ClinVar Variation:

2580859

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Gly227Arg	CA367401116 NM_001354800.1:c.679G>C