Canonical Allele Identifier: PA2825946849
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1481540
ClinVar RCV Id: RCV001988358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala137Thr
CA392238132
NM_001160227.2:c.409G>A