Allele Registry

Canonical Allele Identifier: PA2827616706

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000143817

RCV000790205

RCV000988269

RCV001049421

RCV002326849

ClinVar Variation:

155746

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338456.1:p.Lys1425Glu	CA233102 NM_001351527.2:c.4273A>G