Canonical Allele Identifier: PA916039382
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804833
ClinVar RCV Id: RCV000992035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser53Pro
CA367398853
NM_001354803.2:c.157T>C