Canonical Allele Identifier: PA2825947752
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 999284
ClinVar RCV Id: RCV001295262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Gln1231Arg
CA7534864
NM_001160227.2:c.3692A>G