Allele Registry

Canonical Allele Identifier: PA096934

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000002380

RCV000414273

RCV000789614

ClinVar Variation:

2290

HGVS (amino-acid)	Matching Registered Transcripts
NP_055861.3:p.Thr3Ile	CA252185 NM_015046.7:c.8C>T