Canonical Allele Identifier: PA2825145173
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1038341
ClinVar RCV Id: RCV002254630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000447.2:p.Arg538Gly
CA385298995
NM_000456.3:c.1612C>G