Canonical Allele Identifier: PA353856
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 219179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp345Tyr
CA279947
NM_033507.3:c.1033G>T