Allele Registry

Canonical Allele Identifier: PA118382

Gene: B3GALNT1 HGNC NCBI

ClinVar Allele:

21675

ClinVar RCV:

RCV000007015

ClinVar Variation:

6636

HGVS (amino-acid)	Matching Registered Transcripts
NP_149359.1:p.Glu266Ala	CA118380 NM_033169.3:c.797A>C