Canonical Allele Identifier: PA1139735402
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 910353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Glu99Gly
CA367397281
NM_001354803.2:c.296A>G