Canonical Allele Identifier: PA658661498
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 466541
ClinVar RCV Id: RCV000545580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.His1809Arg
CA392222572
NM_025137.4:c.5426A>G