Canonical Allele Identifier: PA1139735355
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 982610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly63Glu
CA367398712
NM_001354803.2:c.188G>A