Canonical Allele Identifier: PA2580138961
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1980886
ClinVar RCV Id: RCV002761682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ala291Val
CA385288836
NM_001032387.2:c.872C>T