Canonical Allele Identifier: PA2741944015
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2929585
ClinVar RCV Id: RCV003784751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Val1404Ile
CA375326957
NM_015046.7:c.4210G>A