Canonical Allele Identifier: PA2499235859
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1018095
ClinVar RCV Id: RCV002254620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg398Trp
CA6621126
NM_001032387.2:c.1192C>T