Allele Registry

Canonical Allele Identifier: PA2825947169

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000318542

RCV001529614

RCV002402029

ClinVar Variation:

316108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153699.1:p.Leu520Phe	CA7535527 NM_001160227.2:c.1558C>T