Canonical Allele Identifier: PA658672856
Gene: B3GALNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 473879
ClinVar RCV Id: RCV000531674
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689703.1:p.Ile370Phe
CA344957775
NM_152490.5:c.1108A>T