Canonical Allele Identifier: PA2825364440
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1045213
ClinVar RCV Id: RCV002254636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Ile525Val
CA237605366
NM_001032386.2:c.1573A>G