Canonical Allele Identifier: PA2825364295
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309843
ClinVar RCV Id: RCV000328752
ClinVar Variation Id: 1492843
ClinVar RCV Id: RCV001981277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Ala428Thr
CA6621143
NM_001032386.2:c.1282G>A
CA2573148930
NM_001032386.2:c.1281_1282delinsCA