Canonical Allele Identifier: PA2826713979
Gene: B3GAT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472368
ClinVar RCV Id: RCV002002867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275651.1:p.Leu109Val
CA380977219
NM_001288722.1:c.325C>G