Canonical Allele Identifier: PA1139735338
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995100
ClinVar RCV Id: RCV001288973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala62Pro
CA367398729
NM_001354803.2:c.184G>C