Allele Registry

Canonical Allele Identifier: PA2827617767

Gene: SETX HGNC NCBI

ClinVar RCV:

RCV000533100

ClinVar Variation:

468496

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338457.1:p.Thr952Ala	CA375333512 NM_001351528.2:c.2854A>G