Allele Registry

Canonical Allele Identifier: PA2828125462

Gene: SPAST HGNC NCBI

ClinVar RCV:

RCV000585458

RCV001063727

RCV003233753

ClinVar Variation:

493274

857953

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350804.1:p.Ser562Arg	CA346505634 NM_001363875.2:c.1684A>C CA346505640 NM_001363875.2:c.1686C>A CA346505641 NM_001363875.2:c.1686C>G