Canonical Allele Identifier: PA2741997481
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2700200
ClinVar RCV Id: RCV003547122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile160Thr
CA367401855
NM_033507.3:c.479T>C