Canonical Allele Identifier: PA2825382271
Gene: B3GALNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6636
ClinVar RCV Id: RCV000007015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001033717.1:p.Glu266Ala
CA118380
NM_001038628.2:c.797A>C