Allele Registry

Canonical Allele Identifier: PA645408210

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000413070

RCV000713421

RCV001088264

RCV002356511

ClinVar Variation:

373681

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Leu2004Val	CA7534277 NM_025137.4:c.6010T>G