Canonical Allele Identifier: PA2825364893
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 3172135
ClinVar RCV Id: RCV004461077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Cys317Phe
CA6621069
NM_001032387.2:c.950G>T