Canonical Allele Identifier: PA915957657
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309838
ClinVar RCV Id: RCV000302757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg297Trp
CA6621059
NM_001032387.2:c.889C>T