Allele Registry

Canonical Allele Identifier: PA645426298

Gene: SETX HGNC NCBI

ClinVar Variation Id: 285878

HGVS (amino-acid)	Matching Registered Transcripts
NP_055861.3:p.Ser1019Tyr	CA5297486 NM_015046.7:c.3056C>A