Canonical Allele Identifier: PA645387764
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309839
ClinVar RCV Id: RCV000357593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Thr328Ile
CA6621074
NM_000456.3:c.983C>T