Canonical Allele Identifier: PA2825364668
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 3172132
ClinVar RCV Id: RCV004461074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Gly131Ser
CA6620971
NM_001032387.2:c.391G>A