Canonical Allele Identifier: PA2830122744
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1505039
ClinVar RCV Id: RCV002047952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr48Ile
CA367403399
NM_033508.3:c.143C>T