Canonical Allele Identifier: PA2825364262
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1010352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Pro388Thr
CA6621118
NM_001032386.2:c.1162C>A