Canonical Allele Identifier: PA2825948228
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1479215
ClinVar RCV Id: RCV001976668 RCV002573505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ser1833Pro
CA7534397
NM_001160227.2:c.5497T>C