Canonical Allele Identifier: PA658810490
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 536375
ClinVar RCV Id: RCV000644812 RCV002473087 RCV003233770 RCV003233769
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Thr752Ala
CA5297637
NM_015046.7:c.2254A>G