Canonical Allele Identifier: PA2827936603
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1746350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly175Glu
CA367401680
NM_001354800.1:c.524G>A