Allele Registry

Canonical Allele Identifier: PA658661446

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000517770

RCV001851462

RCV002467849

RCV002467850

ClinVar Variation:

448461

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Asp588Gly	CA7535442 NM_025137.4:c.1763A>G