Canonical Allele Identifier: PA2573260528
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1405665
ClinVar RCV Id: RCV001906619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Gly382Ala
CA346501290
NM_014946.4:c.1145G>C