Allele Registry

Canonical Allele Identifier: PA344328

Gene: SPG11 HGNC NCBI

ClinVar Allele:

49722

ClinVar RCV:

RCV000034199

ClinVar Variation:

41298

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Arg945Gly	CA344327 NM_025137.4:c.2833A>G