Canonical Allele Identifier: PA118382
Gene: B3GALNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6636
ClinVar RCV Id: RCV000007015
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Amino-acid Alleles

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