Canonical Allele Identifier: PA2828733402
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 432722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg399Gln
CA346502079
NM_001377959.1:c.1196G>A