Canonical Allele Identifier: PA2830124072
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala448Thr
CA213758
NM_033508.3:c.1342G>A