Canonical Allele Identifier: PA2825948223
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 965841
ClinVar RCV Id: RCV001240382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Thr1828Ala
CA392222448
NM_001160227.2:c.5482A>G