Canonical Allele Identifier: PA2580138963
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2109278
ClinVar RCV Id: RCV003038277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ala294Asp
CA385288919
NM_001032387.2:c.881C>A