Canonical Allele Identifier: PA2827936946
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Cys382Arg
CA367398754
NM_001354800.1:c.1144T>C