Canonical Allele Identifier: PA916055796
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 646208
ClinVar RCV Id: RCV000800444
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Arg1813Gly
CA392222549
NM_025137.4:c.5437A>G