Canonical Allele Identifier: PA645460265
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 418226
ClinVar RCV Id: RCV000482178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val254Ile
CA4239529
NM_033507.3:c.760G>A