Canonical Allele Identifier: PA2741988121
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613197
ClinVar RCV Id: RCV003373876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ile1801Asn
CA392222619
NM_025137.4:c.5402T>A