Canonical Allele Identifier: PA2573288996
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349205
ClinVar RCV Id: RCV002051000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Glu1831Gly
CA392222428
NM_025137.4:c.5492A>G