Canonical Allele Identifier: PA2828119170
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 417627
ClinVar RCV Id: RCV000468399
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Asp492Tyr
CA16616712
NM_001363823.2:c.1474G>T