Canonical Allele Identifier: PA2825946818
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 284018
ClinVar RCV Id: RCV000296854 RCV000692595 RCV002321952 RCV002467713 RCV002467714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala106Thr
CA7535871
NM_001160227.2:c.316G>A