Canonical Allele Identifier: PA2825948214
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396576
ClinVar RCV Id: RCV001887452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Glu1817Gly
CA392222516
NM_001160227.2:c.5450A>G