Canonical Allele Identifier: PA2830122399
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2571660
ClinVar RCV Id: RCV003313370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe420Val
CA367397313
NM_033507.3:c.1258T>G