Canonical Allele Identifier: PA658668956
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe149Ile
CA367401967
NM_033507.3:c.445T>A