Allele Registry

Canonical Allele Identifier: PA658661407

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000548900

RCV003962530

ClinVar Variation:

466529

HGVS (amino-acid)	Matching Registered Transcripts
NP_079413.3:p.Asp146Gly	CA7535844 NM_025137.4:c.437A>G