Canonical Allele Identifier: PA2826573688
Gene: B3GALNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153976
ClinVar RCV Id: RCV003081556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264084.1:p.His138Arg
CA344928611
NM_001277155.3:c.413A>G