Canonical Allele Identifier: PA915957673
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309843
ClinVar RCV Id: RCV000328752
ClinVar Variation Id: 1492843
ClinVar RCV Id: RCV001981277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ala428Thr
CA6621143
NM_001032387.2:c.1282G>A
CA2573148930
NM_001032387.2:c.1281_1282delinsCA