Canonical Allele Identifier: PA658661496
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 466539
ClinVar RCV Id: RCV000553692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Arg1805His
CA7534410
NM_025137.4:c.5414G>A