Canonical Allele Identifier: PA2830123870
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1734018
ClinVar RCV Id: RCV002348865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala383Thr
CA367398732
NM_033508.3:c.1147G>A