Canonical Allele Identifier: PA915957686
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 3823
ClinVar RCV Id: RCV000758702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Gly530Asp
CA116471
NM_001032387.2:c.1589G>A