Canonical Allele Identifier: PA645459517
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser132Pro
CA126213
NM_033507.3:c.394T>C