Canonical Allele Identifier: PA915957671
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309841
ClinVar RCV Id: RCV000322978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ser416Phe
CA10642061
NM_001032387.2:c.1247C>T