Allele Registry

Canonical Allele Identifier: PA1139723967

Gene: SPAST HGNC NCBI

ClinVar RCV:

RCV001268059

ClinVar Variation:

986901

HGVS (amino-acid)	Matching Registered Transcripts
NP_055761.2:p.Leu371Val	CA346501218 NM_014946.4:c.1111C>G