Canonical Allele Identifier: PA2830122018
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr363Ile
CA367399081
NM_033507.3:c.1088C>T