Allele Registry

Canonical Allele Identifier: PA658662238

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000515884

RCV000560688

RCV000859602

RCV001169791

RCV001169792

RCV002356794

RCV004541530

ClinVar Variation:

424692

HGVS (amino-acid)	Matching Registered Transcripts
NP_055861.3:p.Gln1276Glu	CA5297318 NM_015046.7:c.3826C>G