Allele Registry

Canonical Allele Identifier: PA658662161

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000517524

RCV001039811

RCV001168904

RCV001168905

RCV002223857

RCV002420301

ClinVar Variation:

448351

HGVS (amino-acid)	Matching Registered Transcripts
NP_055861.3:p.Ser269Leu	CA5297936 NM_015046.7:c.806C>T