Canonical Allele Identifier: PA2579980678
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys371Trp
CA367398928
NM_000162.5:c.1113C>G