Allele Registry

Canonical Allele Identifier: PA351261

Gene: B3GALNT2 HGNC NCBI

ClinVar RCV:

RCV001854841

ClinVar Variation:

242531

HGVS (amino-acid)	Matching Registered Transcripts
NP_689703.1:p.Asp327Asn	CA351260 NM_152490.5:c.979G>A