Canonical Allele Identifier: PA2573288969
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396576
ClinVar RCV Id: RCV001887452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Glu1817Gly
CA392222516
NM_025137.4:c.5450A>G