Canonical Allele Identifier: PA096188
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 217004
ClinVar RCV Id: RCV000195806 RCV001091364 RCV003401083 RCV001847904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Arg562Gln
CA278930
NM_014946.4:c.1685G>A