Allele Registry

Canonical Allele Identifier: PA2825946860

Gene: SPG11 HGNC NCBI

ClinVar RCV:

RCV000548900

RCV003962530

ClinVar Variation:

466529

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153699.1:p.Asp146Gly	CA7535844 NM_001160227.2:c.437A>G