Canonical Allele Identifier: PA2828119079
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 432722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg430Gln
CA346502079
NM_001363823.2:c.1289G>A