Canonical Allele Identifier: PA2830123845
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys381Arg
CA367398754
NM_033508.3:c.1141T>C