Allele Registry

Canonical Allele Identifier: PA916030109

Gene: B3GALNT1 HGNC NCBI

ClinVar RCV:

RCV000007015

ClinVar Variation:

6636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336092.1:p.Glu386Ala	CA118380 NM_001349163.2:c.1157A>C