Canonical Allele Identifier: PA2828119036
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ile405Val
CA253568
NM_001363823.2:c.1213A>G