Canonical Allele Identifier: PA2499235867
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1045213
ClinVar RCV Id: RCV002254636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ile525Val
CA237605366
NM_001032387.2:c.1573A>G