Canonical Allele Identifier: PA2741868033
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2767216
ClinVar RCV Id: RCV003573794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser53Tyr
CA367398843
NM_001354803.2:c.158C>A