Canonical Allele Identifier: PA915957684
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 802865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Asp512Tyr
CA6621176
NM_001032387.2:c.1534G>T