Canonical Allele Identifier: PA2580467760
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1896712
ClinVar RCV Id: RCV002569779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Arg1805Pro
CA392222594
NM_025137.4:c.5414G>C