Canonical Allele Identifier: PA658662278
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 448338
ClinVar RCV Id: RCV000518592 RCV002525079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Asn1935Ser
CA5296892
NM_015046.7:c.5804A>G