Canonical Allele Identifier: PA2499252078
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Cys60Tyr
CA367398751
NM_001354803.2:c.179G>A