Allele Registry

Canonical Allele Identifier: PA2828119042

Gene: SPAST HGNC NCBI

ClinVar Variation Id: 1452772

ClinVar RCV Id: RCV002037743

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350752.1:p.Ala408Glu	CA346501477 NM_001363823.2:c.1223C>A