Allele Registry

Canonical Allele Identifier: PA2827617635

Gene: SETX HGNC NCBI

ClinVar Variation Id: 468490

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338457.1:p.Asn669Tyr	CA5297680 NM_001351528.2:c.2005A>T