Allele Registry

Canonical Allele Identifier: PA2499291648

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV001305008

ClinVar Variation:

1007774

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Arg2034Gly	CA7534262 NM_025137.4:c.6100C>G