Canonical Allele Identifier: PA2830441067
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1363767
ClinVar RCV Id: RCV001905076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Pro403Leu
CA346502105
NM_199436.2:c.1208C>T