Canonical Allele Identifier: PA2825946814
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344087
ClinVar RCV Id: RCV001848190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Thr99Ala
CA392238386
NM_001160227.2:c.295A>G