Canonical Allele Identifier: PA915957645
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 309833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Arg76Ser
CA6620904
NM_001032387.2:c.228G>T
CA385279967
NM_001032387.2:c.228G>C