Allele Registry

Canonical Allele Identifier: PA2828118967

Gene: SPAST HGNC NCBI

ClinVar Allele:

20696

ClinVar RCV:

RCV000006011

ClinVar Variation:

5657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350752.1:p.Ser361Cys	CA253546 NM_001363823.2:c.1082C>G