Canonical Allele Identifier: PA2825948202
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1896712
ClinVar RCV Id: RCV002569779
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg1805Pro
CA392222594
NM_001160227.2:c.5414G>C