Canonical Allele Identifier: PA2825144962
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2089056
ClinVar RCV Id: RCV003011951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Gly295Ala
CA385288954
NM_000456.3:c.884G>C