Canonical Allele Identifier: PA2825947517
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 41298
ClinVar RCV Id: RCV000034199
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg945Gly
CA344327
NM_001160227.2:c.2833A>G