Canonical Allele Identifier: PA915957646
Gene: SUOX HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Val111Asp
CA203849
NM_001032387.2:c.332T>A