Canonical Allele Identifier: PA891855880
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 571323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Arg1824Gln
CA7534402
NM_025137.4:c.5471G>A