Allele Registry

Canonical Allele Identifier: PA2828733307

Gene: SPAST HGNC NCBI

ClinVar RCV:

RCV001268059

ClinVar Variation:

986901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364888.1:p.Leu339Val	CA346501218 NM_001377959.1:c.1015C>G