Canonical Allele Identifier: PA2580383041
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2125906
ClinVar RCV Id: RCV003043857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Gly419Val
CA346501856
NM_014946.4:c.1256G>T