Canonical Allele Identifier: PA2825946808
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1434058
ClinVar RCV Id: RCV001984524 RCV003136336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg93His
CA7535879
NM_001160227.2:c.278G>A