Canonical Allele Identifier: PA891855879
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 586643
ClinVar RCV Id: RCV000713420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Asn1814Tyr
CA392222542
NM_025137.4:c.5440A>T