Canonical Allele Identifier: PA2828119082
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1709809
ClinVar RCV Id: RCV002290151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro434Thr
CA346502103
NM_001363823.2:c.1300C>A