Canonical Allele Identifier: PA2827936778
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16135
ClinVar Variation Id: 447418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly261Arg
CA126211
NM_001354800.1:c.781G>A
CA367400571
NM_001354800.1:c.781G>C