Canonical Allele Identifier: PA2825948222
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007005
ClinVar RCV Id: RCV001304128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ile1826Val
CA392222461
NM_001160227.2:c.5476A>G