Allele Registry

Canonical Allele Identifier: PA2825947241

Gene: SPG11 HGNC NCBI

ClinVar Allele:

339012

ClinVar RCV:

RCV000558428

RCV002244797

RCV002411207

ClinVar Variation:

316106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153699.1:p.Pro601Thr	CA7535435 NM_001160227.2:c.1801C>A