Canonical Allele Identifier: PA2573174954
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1462267
ClinVar RCV Id: RCV001985652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg292His
CA6621058
NM_001032387.2:c.875G>A