Canonical Allele Identifier: PA2830123109
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe149Tyr
CA231135
NM_033508.3:c.446T>A