Canonical Allele Identifier: PA916030109
Gene: B3GALNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6636
ClinVar RCV Id: RCV000007015
JSON-LD

Amino-acid Alleles

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