Canonical Allele Identifier: PA658810267
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536437
ClinVar RCV Id: RCV000644887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro374Leu
CA346501238
NM_014946.4:c.1121C>T