Canonical Allele Identifier: PA658669138
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Cys383Arg
CA367398754
NM_033507.3:c.1147T>C