Canonical Allele Identifier: PA915972930
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 653482
ClinVar RCV Id: RCV000809266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Val1319Ile
CA5297297
NM_015046.7:c.3955G>A