Canonical Allele Identifier: PA645387790
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Arg529Gln
CA6621186
NM_000456.3:c.1586G>A