Canonical Allele Identifier: PA891855873
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 566662
ClinVar RCV Id: RCV000686533 RCV000995317 RCV002468000 RCV002343435 RCV002467999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.His1757Arg
CA7534436
NM_025137.4:c.5270A>G