Canonical Allele Identifier: PA2825948189
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195581
ClinVar RCV Id: RCV002628783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Glu1796_Glu1798dup
CA618005996
NM_001160227.2:c.5386_5394dup