Canonical Allele Identifier: PA2830122248
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1301416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg393Gly
CA367398625
NM_033507.3:c.1177C>G