Canonical Allele Identifier: PA916039408
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Lys92Glu
CA213739
NM_001354803.2:c.274A>G