Allele Registry

Canonical Allele Identifier: PA2827463432

Gene: B3GALNT1 HGNC NCBI

ClinVar RCV:

RCV000007015

ClinVar Variation:

6636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336075.1:p.Glu266Ala	CA118380 NM_001349146.2:c.797A>C