Canonical Allele Identifier: PA2580467892
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2014937
ClinVar RCV Id: RCV002861733
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ser1961Gly
CA392219181
NM_025137.4:c.5881A>G