Canonical Allele Identifier: PA2830123755
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 219179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp343Tyr
CA279947
NM_033508.3:c.1027G>T