Canonical Allele Identifier: PA2825946859
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 859288
ClinVar RCV Id: RCV001065361 RCV002553973
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Gln145Arg
CA7535847
NM_001160227.2:c.434A>G