Canonical Allele Identifier: PA2825144837
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 957842
ClinVar RCV Id: RCV002254604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Pro162Leu
CA385283993
NM_000456.3:c.485C>T