Canonical Allele Identifier: PA2825946898
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 316114
ClinVar RCV Id: RCV000348489 RCV002467754 RCV002467755
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Pro194Leu
CA7535791
NM_001160227.2:c.581C>T