Canonical Allele Identifier: PA2499235869
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1038341
ClinVar RCV Id: RCV002254630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg538Gly
CA385298995
NM_001032387.2:c.1612C>G