Canonical Allele Identifier: PA916039387
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala56Val
CA341585
NM_001354803.2:c.167C>T