Allele Registry

Canonical Allele Identifier: PA2825947680

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000517057

RCV000840197

RCV001084485

RCV002455996

ClinVar Variation:

448466

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