Canonical Allele Identifier: PA2573071451
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1300949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val86Met
CA367398343
NM_001354803.2:c.256G>A