Canonical Allele Identifier: PA645472392
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 409032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ala495Thr
CA16610831
NM_014946.4:c.1483G>A