Allele Registry

Canonical Allele Identifier: PA2827617671

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000644812

RCV002473087

RCV003233769

RCV003233770

ClinVar Variation:

536375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338457.1:p.Thr752Ala	CA5297637 NM_001351528.2:c.2254A>G