Canonical Allele Identifier: PA2499235842
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1058415
ClinVar RCV Id: RCV002254643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Thr172Ala
CA6620995
NM_001032387.2:c.514A>G