Canonical Allele Identifier: PA2825365073
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 3172131
ClinVar RCV Id: RCV004461073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Pro496Ser
CA385297339
NM_001032387.2:c.1486C>T