Allele Registry

Canonical Allele Identifier: PA2828733085

Gene: SPAST HGNC NCBI

ClinVar Variation Id: 1969356

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364888.1:p.Phe75Leu	CA45201396 NM_001377959.1:c.225C>A CA346601767 NM_001377959.1:c.223T>C CA346601783 NM_001377959.1:c.225C>G