Canonical Allele Identifier: PA2825948103
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 219558
ClinVar RCV Id: RCV000206755 RCV001331382 RCV002467666 RCV002336551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala1687Thr
CA350762
NM_001160227.2:c.5059G>A