Canonical Allele Identifier: PA2826573684
Gene: B3GALNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 968878
ClinVar RCV Id: RCV001244113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264084.1:p.Val131Leu
CA1464952
NM_001277155.3:c.391G>C
CA1464953
NM_001277155.3:c.391G>T