Canonical Allele Identifier: PA2825145112
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1304091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Asp461Val
CA6621161
NM_000456.3:c.1382A>T