Canonical Allele Identifier: PA2825946818
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 284018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala106Thr
CA7535871
NM_001160227.2:c.316G>A