Canonical Allele Identifier: PA915957680
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 638376
ClinVar RCV Id: RCV000791011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg459Gln
CA6621160
NM_001032387.2:c.1376G>A