Canonical Allele Identifier: PA2825364181
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1064322
ClinVar RCV Id: RCV002254648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Arg292Cys
CA6621057
NM_001032386.2:c.874C>T