Canonical Allele Identifier: PA203850
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 202185
ClinVar RCV Id: RCV000184031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Val111Asp
CA203849
NM_000456.3:c.332T>A