Canonical Allele Identifier: PA2825946806
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717020
ClinVar RCV Id: RCV002296210
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Asp91Tyr
CA392238436
NM_001160227.2:c.271G>T