Allele Registry

Canonical Allele Identifier: PA916008107

Gene: B3GALNT2 HGNC NCBI

ClinVar RCV:

RCV000034847

RCV000119388

ClinVar Variation:

41937

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264084.1:p.Val293Gly	CA231751 NM_001277155.3:c.878T>G