Canonical Allele Identifier: PA2580467763
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202423
ClinVar RCV Id: RCV002647984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Leu1811Pro
CA392222557
NM_025137.4:c.5432T>C