Canonical Allele Identifier: PA2830123563
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16135
ClinVar Variation Id: 447418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly260Arg
CA126211
NM_033508.3:c.778G>A
CA367400571
NM_033508.3:c.778G>C