Canonical Allele Identifier: PA2830124042
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679548
ClinVar RCV Id: RCV002227427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe437Val
CA367397071
NM_033508.3:c.1309T>G