Canonical Allele Identifier: PA2825145136
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1018855
ClinVar RCV Id: RCV002254621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Pro496Arg
CA385297346
NM_000456.3:c.1487C>G