Canonical Allele Identifier: PA2580390532
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2418133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Arg1294His
CA5297312
NM_015046.7:c.3881G>A