Canonical Allele Identifier: PA1139759706
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 859288
ClinVar RCV Id: RCV001065361 RCV002553973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Gln145Arg
CA7535847
NM_025137.4:c.434A>G