Canonical Allele Identifier: PA645460298
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg276Leu
CA367400477
NM_033507.3:c.827G>T