Canonical Allele Identifier: PA2580523212
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_689703.1:p.His97Arg
CA344928611
NM_152490.5:c.290A>G