Canonical Allele Identifier: PA2580139016
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2013652
ClinVar RCV Id: RCV002834828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Ala428Pro
CA385292987
NM_001032387.2:c.1282G>C
CA2580086510
NM_001032387.2:c.1281_1282delinsCC