Canonical Allele Identifier: PA2825947011
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 284761
ClinVar RCV Id: RCV000259263 RCV000811912 RCV002467716 RCV002379128 RCV002467715
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Leu327Val
CA7535662
NM_001160227.2:c.979C>G