Canonical Allele Identifier: PA356384
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 219558
ClinVar RCV Id: RCV000206755 RCV001331382 RCV002467666 RCV002336551
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ala1687Thr
CA350762
NM_025137.4:c.5059G>A