Canonical Allele Identifier: PA2825946810
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069015
ClinVar RCV Id: RCV002975275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg93Leu
CA392238422
NM_001160227.2:c.278G>T