Canonical Allele Identifier: PA152951
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys371Phe
CA152950
NM_000162.5:c.1112G>T