Canonical Allele Identifier: PA2825946821
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 241592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Asn110Asp
CA7535868
NM_001160227.2:c.328A>G