Allele Registry

Canonical Allele Identifier: PA2828120897

Gene: SPG7 HGNC NCBI

ClinVar Allele:

211751

ClinVar RCV:

RCV000197675

RCV001039520

RCV002515438

ClinVar Variation:

215207

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350779.1:p.Thr261Met	CA322133 NM_001363850.1:c.782C>T