Canonical Allele Identifier: PA915957646
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_001027559.1:p.Val111Asp
CA203849
NM_001032387.2:c.332T>A