Canonical Allele Identifier: PA2828119023
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1311513
ClinVar RCV Id: RCV001752496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ala393Val
CA346501378
NM_001363823.2:c.1178C>T