Allele Registry

Canonical Allele Identifier: PA2741997602

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003330054

ClinVar Variation:

2580859

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly228Arg	CA367401116 NM_033507.3:c.682G>C