Canonical Allele Identifier: PA1139673674
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 862847
ClinVar RCV Id: RCV001069660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg297Gln
CA6621060
NM_001032387.2:c.890G>A