Canonical Allele Identifier: PA2825948424
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 581478
ClinVar RCV Id: RCV000705312 RCV002360824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Gly2044Glu
CA392216243
NM_001160227.2:c.6131G>A