Allele Registry

Canonical Allele Identifier: PA658662187

Gene: SETX HGNC NCBI

ClinVar Variation Id: 468490

HGVS (amino-acid)	Matching Registered Transcripts
NP_055861.3:p.Asn669Tyr	CA5297680 NM_015046.7:c.2005A>T