Canonical Allele Identifier: PA2825948226
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349205
ClinVar RCV Id: RCV002051000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Glu1831Gly
CA392222428
NM_001160227.2:c.5492A>G