Allele Registry

Canonical Allele Identifier: PA2825947452

Gene: SPG11 HGNC NCBI

ClinVar Allele:

49717

ClinVar RCV:

RCV000034194

ClinVar Variation:

41293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153699.1:p.Ile870Val	CA344320 NM_001160227.2:c.2608A>G