Canonical Allele Identifier: PA2825947557
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 574531
ClinVar RCV Id: RCV000696485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Lys983Ile
CA392229414
NM_001160227.2:c.2948A>T