Canonical Allele Identifier: PA2828733465
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5670
ClinVar RCV Id: RCV000006024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Asp438Val
CA253564
NM_001377959.1:c.1313A>T