Canonical Allele Identifier: PA2828118686
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 391244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro33Leu
CA1600482
NM_001363823.2:c.98C>T