Canonical Allele Identifier: PA111131
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 3823
ClinVar RCV Id: RCV000758702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Gly530Asp
CA116471
NM_000456.3:c.1589G>A