Canonical Allele Identifier: PA645460193
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 283358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg192Gln
CA10604473
NM_033507.3:c.575G>A