Canonical Allele Identifier: PA2499252079
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser61Pro
CA367398737
NM_001354803.2:c.181T>C