Canonical Allele Identifier: PA2828119029
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448442
ClinVar RCV Id: RCV000516537 RCV000686298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ser398Leu
CA346501410
NM_001363823.2:c.1193C>T