Canonical Allele Identifier: PA2825948207
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 963641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Thr1810Ser
CA392222564
NM_001160227.2:c.5429C>G
CA392222565
NM_001160227.2:c.5428A>T