Canonical Allele Identifier: PA2828118760
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1344060
ClinVar RCV Id: RCV001848163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro97Arg
CA346602138
NM_001363823.2:c.290C>G