Canonical Allele Identifier: PA111096
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 986985
ClinVar RCV Id: RCV001268179 RCV002290677 RCV003492239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Arg366His
CA6621097
NM_000456.3:c.1097G>A