Canonical Allele Identifier: PA2825075892
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1343440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr60Ile
CA4239709
NM_000162.5:c.179C>T