Allele Registry

Canonical Allele Identifier: PA344319

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000034192

ClinVar Variation:

41291

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Arg815Met	CA344318 NM_025137.4:c.2444G>T