Canonical Allele Identifier: PA2825946834
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733057
ClinVar RCV Id: RCV002455173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Leu120Ser
CA392238248
NM_001160227.2:c.359T>C