Canonical Allele Identifier: PA2828119056
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 586659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Val415Ala
CA346501824
NM_001363823.2:c.1244T>C