Canonical Allele Identifier: PA2827617964
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2418133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Arg1294His
CA5297312
NM_001351528.2:c.3881G>A