Canonical Allele Identifier: PA916039389
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala57Val
CA367398790
NM_001354803.2:c.170C>T