Canonical Allele Identifier: PA2499235858
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1022885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Tyr392Cys
CA6621121
NM_001032387.2:c.1175A>G