Canonical Allele Identifier: PA916039402
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg70Leu
CA213733
NM_001354803.2:c.209G>T