Allele Registry

Canonical Allele Identifier: PA355769

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000205403

RCV000995316

RCV002354579

RCV002467667

RCV002467668

ClinVar Variation:

220392

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Arg2031Gly	CA349566 NM_025137.4:c.6091C>G