Canonical Allele Identifier: PA2579982247
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg155Thr
CA367401902
NM_000162.5:c.464G>C