Canonical Allele Identifier: PA2825948231
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063487
ClinVar RCV Id: RCV001373326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala1838Pro
CA7534396
NM_001160227.2:c.5512G>C