Canonical Allele Identifier: PA2828119077
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Leu425Phe
CA346502047
NM_001363823.2:c.1273C>T