Canonical Allele Identifier: PA2825948198
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613197
ClinVar RCV Id: RCV003373876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ile1801Asn
CA392222619
NM_001160227.2:c.5402T>A