Canonical Allele Identifier: PA2825946803
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 851486
ClinVar RCV Id: RCV001055894
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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