Canonical Allele Identifier: PA916039384
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg55Cys
CA367398826
NM_001354803.2:c.163C>T