Allele Registry

Canonical Allele Identifier: PA201296

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000175101

RCV000204165

RCV001260215

RCV001847810

RCV002262769

ClinVar Variation:

194676

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Lys1013Glu	CA201295 NM_025137.4:c.3037A>G