Canonical Allele Identifier: PA2580138906
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1811837
ClinVar RCV Id: RCV002510256 RCV002571586 RCV002571587 RCV003971303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.His118Tyr
CA6620963
NM_001032387.2:c.352C>T