Canonical Allele Identifier: PA101250
Gene: B3GALNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41937
ClinVar RCV Id: RCV000034847 RCV000119388
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689703.1:p.Val252Gly
CA231751
NM_152490.5:c.755T>G