Canonical Allele Identifier: PA2825144771
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1513545
ClinVar RCV Id: RCV002045936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Val90Leu
CA385282065
NM_000456.3:c.268G>C
CA385282066
NM_000456.3:c.268G>T