Canonical Allele Identifier: PA2830123848
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1256304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys381Tyr
CA367398751
NM_033508.3:c.1142G>A