Allele Registry

Canonical Allele Identifier: PA916008104

Gene: B3GALNT2 HGNC NCBI

ClinVar RCV:

RCV000490097

ClinVar Variation:

427099

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264084.1:p.Gly289Ala	CA1464816 NM_001277155.3:c.866G>C