Canonical Allele Identifier: PA2573296395
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1505039
ClinVar RCV Id: RCV002047952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr50Ile
CA367403399
NM_033507.3:c.149C>T