Canonical Allele Identifier: PA2828733413
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Asp409Gly
CA253555
NM_001377959.1:c.1226A>G