Canonical Allele Identifier: PA2830122764
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Lys55Thr
CA367403326
NM_033508.3:c.164A>C