Allele Registry

Canonical Allele Identifier: PA2828120921

Gene: SPG7 HGNC NCBI

ClinVar Allele:

401888

ClinVar RCV:

RCV000461245

ClinVar Variation:

411681

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350779.1:p.Val311Glu	CA16615322 NM_001363850.1:c.932T>A