Canonical Allele Identifier: PA344328
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 41298
ClinVar RCV Id: RCV000034199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Arg945Gly
CA344327
NM_025137.4:c.2833A>G