Canonical Allele Identifier: PA2580139002
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2137377
ClinVar RCV Id: RCV003062521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Lys379Arg
CA6621114
NM_001032387.2:c.1136A>G