Canonical Allele Identifier: PA2825947241
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 316106
ClinVar RCV Id: RCV000558428 RCV002244797 RCV002411207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Pro601Thr
CA7535435
NM_001160227.2:c.1801C>A