Allele Registry

Canonical Allele Identifier: PA645426275

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000344541

RCV000390382

RCV000803584

ClinVar Variation:

365368

HGVS (amino-acid)	Matching Registered Transcripts
NP_055861.3:p.Asn668Ser	CA5297681 NM_015046.7:c.2003A>G