Canonical Allele Identifier: PA2580139005
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1717586
ClinVar RCV Id: RCV002296477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Val386Met
CA6621117
NM_001032387.2:c.1156G>A