Canonical Allele Identifier: PA1139758441
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 897739
ClinVar RCV Id: RCV001141201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.His46Arg
CA1600500
NM_199436.2:c.137A>G