Canonical Allele Identifier: PA645387762
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309838
ClinVar RCV Id: RCV000302757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Arg297Trp
CA6621059
NM_000456.3:c.889C>T