Canonical Allele Identifier: PA2830122777
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1343440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr59Ile
CA4239709
NM_033508.3:c.176C>T