Canonical Allele Identifier: PA2829789241
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1901782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro25Ala
CA346601307
NM_014946.4:c.73C>G