Allele Registry

Canonical Allele Identifier: PA2828733349

Gene: SPAST HGNC NCBI

ClinVar Allele:

451187

ClinVar RCV:

RCV000536355

ClinVar Variation:

468561

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364888.1:p.Ser367Trp	CA346501409 NM_001377959.1:c.1100C>G