Canonical Allele Identifier: PA2827618048
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2926433
ClinVar RCV Id: RCV003786719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Val1451Glu
CA375326443
NM_001351528.2:c.4352T>A