Canonical Allele Identifier: PA891850233
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 576378
ClinVar RCV Id: RCV002254570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Glu311Lys
CA6621065
NM_000456.3:c.931G>A