Canonical Allele Identifier: PA2825947758
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 466525
ClinVar RCV Id: RCV000560585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ile1240Thr
CA270092832
NM_001160227.2:c.3719T>C