Canonical Allele Identifier: PA2825948423
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717261
ClinVar RCV Id: RCV002297475
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Tyr2043Cys
CA392216250
NM_001160227.2:c.6128A>G