Canonical Allele Identifier: PA2825364058
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2016008
ClinVar RCV Id: RCV002846642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027558.1:p.Asn161Lys
CA385283972
NM_001032386.2:c.483T>G
CA385283974
NM_001032386.2:c.483T>A