Allele Registry

Canonical Allele Identifier: PA2828118983

Gene: SPAST HGNC NCBI

ClinVar RCV:

RCV001268059

ClinVar Variation:

986901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350752.1:p.Leu370Val	CA346501218 NM_001363823.2:c.1108C>G