Canonical Allele Identifier: PA891847866
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 566837
ClinVar RCV Id: RCV000686755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Leu380Pro
CA346501275
NM_014946.4:c.1139T>C