Allele Registry

Canonical Allele Identifier: PA2827616701

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000143816

RCV000790204

RCV000988270

RCV001002069

RCV001041860

RCV001167322

RCV002326848

RCV004532621

ClinVar Variation:

155745

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338456.1:p.Asn1409Tyr	CA233099 NM_001351527.2:c.4225A>T