Allele Registry

Canonical Allele Identifier: PA2829789290

Gene: SPAST HGNC NCBI

ClinVar Variation Id: 1707912

HGVS (amino-acid)	Matching Registered Transcripts
NP_055761.2:p.Phe61Leu	CA346601599 NM_014946.4:c.181T>C CA346601609 NM_014946.4:c.183C>A CA346601611 NM_014946.4:c.183C>G