Canonical Allele Identifier: PA915957659
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 596740
ClinVar RCV Id: RCV000732664 RCV002254572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ser323Leu
CA6621070
NM_001032387.2:c.968C>T