Canonical Allele Identifier: PA645460286
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16135
ClinVar Variation Id: 447418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly262Arg
CA126211
NM_033507.3:c.784G>A
CA367400571
NM_033507.3:c.784G>C