Canonical Allele Identifier: PA2825948220
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 571323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg1824Gln
CA7534402
NM_001160227.2:c.5471G>A