Canonical Allele Identifier: PA1139735376
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg75His
CA367398533
NM_001354803.2:c.224G>A