Canonical Allele Identifier: PA2825948209
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202423
ClinVar RCV Id: RCV002647984
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Leu1811Pro
CA392222557
NM_001160227.2:c.5432T>C