Canonical Allele Identifier: PA891847883
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 586659
ClinVar RCV Id: RCV000713463 RCV002298751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Val416Ala
CA346501824
NM_014946.4:c.1247T>C