Canonical Allele Identifier: PA2828733373
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 645183
ClinVar RCV Id: RCV000799219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ser381Leu
CA346501504
NM_001377959.1:c.1142C>T