Canonical Allele Identifier: PA2825364377
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1018855
ClinVar RCV Id: RCV002254621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Pro496Arg
CA385297346
NM_001032386.2:c.1487C>G