Canonical Allele Identifier: PA2827937064
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala449Thr
CA213758
NM_001354800.1:c.1345G>A