Canonical Allele Identifier: PA2573260562
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1452772
ClinVar RCV Id: RCV002037743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ala409Glu
CA346501477
NM_014946.4:c.1226C>A