Allele Registry

Canonical Allele Identifier: PA2827617069

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000002376

ClinVar Variation:

2286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338456.1:p.Pro2213Leu	CA252178 NM_001351527.2:c.6638C>T