Canonical Allele Identifier: PA645387772
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 284923
ClinVar RCV Id: RCV000380532 RCV001859609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Arg433Gln
CA6621145
NM_000456.3:c.1298G>A