Allele Registry

Canonical Allele Identifier: PA2825947573

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000175101

RCV000204165

RCV001260215

RCV001847810

RCV002262769

ClinVar Variation:

194676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153699.1:p.Lys1013Glu	CA201295 NM_001160227.2:c.3037A>G