Canonical Allele Identifier: PA2573174986
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1511573
ClinVar RCV Id: RCV002016817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Val460Met
CA385294140
NM_001032387.2:c.1378G>A