Canonical Allele Identifier: PA2579982028
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg392Pro
CA367398617
NM_000162.5:c.1175G>C