Allele Registry

Canonical Allele Identifier: PA2828733138

Gene: SPAST HGNC NCBI

ClinVar Variation Id: 1298799

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364888.1:p.Phe124Leu	CA346602417 NM_001377959.1:c.370T>C CA346602421 NM_001377959.1:c.372C>A CA346602422 NM_001377959.1:c.372C>G