Canonical Allele Identifier: PA2825947753
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 569104
ClinVar RCV Id: RCV000689647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Gln1232Arg
CA7534863
NM_001160227.2:c.3695A>G