Canonical Allele Identifier: PA2825364063
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1055636
ClinVar RCV Id: RCV002254641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Val166Ile
CA385284090
NM_001032386.2:c.496G>A