Canonical Allele Identifier: PA2825145080
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2013652
ClinVar RCV Id: RCV002834828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Ala428Pro
CA385292987
NM_000456.3:c.1282G>C
CA2580086510
NM_000456.3:c.1281_1282delinsCC