Canonical Allele Identifier: PA2573174918
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1399892
ClinVar RCV Id: RCV001925027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Gln79His
CA237605105
NM_001032387.2:c.237G>C
CA385281739
NM_001032387.2:c.237G>T