Canonical Allele Identifier: PA2825948203
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1747387
ClinVar RCV Id: RCV002349439 RCV003096727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg1805Cys
CA392222597
NM_001160227.2:c.5413C>T