Canonical Allele Identifier: PA2825947680
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 448466
ClinVar RCV Id: RCV000517057 RCV000840197 RCV001084485 RCV002455996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ile1146Val
CA7534984
NM_001160227.2:c.3436A>G