Canonical Allele Identifier: PA2828118801
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1256246
ClinVar RCV Id: RCV001663588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ile129Val
CA346602452
NM_001363823.2:c.385A>G