Canonical Allele Identifier: PA2825946803
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 851486
ClinVar RCV Id: RCV001055894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Trp89Arg
CA7535884
NM_001160227.2:c.265T>C
CA392238448
NM_001160227.2:c.265T>A