Canonical Allele Identifier: PA2827936442
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1343440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr60Ile
CA4239709
NM_001354800.1:c.179C>T