Canonical Allele Identifier: PA2825948264
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2147317
ClinVar RCV Id: RCV003060837
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ile1882Ser
CA7534377
NM_001160227.2:c.5645T>G