Allele Registry

Canonical Allele Identifier: PA2828733466

Gene: SPAST HGNC NCBI

ClinVar RCV:

RCV000526604

ClinVar Variation:

468565

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364888.1:p.Gly439Asp	CA346502364 NM_001377959.1:c.1316G>A CA2586964768 NM_001377959.1:c.1316_1317delinsAC