Canonical Allele Identifier: PA2828733399
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448444
ClinVar RCV Id: RCV000626922 RCV000644897 RCV003482273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Leu394Phe
CA346502047
NM_001377959.1:c.1180C>T