Canonical Allele Identifier: PA2573174973
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1421786
ClinVar RCV Id: RCV001919209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg397Gln
CA237605294
NM_001032387.2:c.1190G>A