Canonical Allele Identifier: PA2825947962
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 534855
ClinVar RCV Id: RCV000642552 RCV001508756 RCV002467957 RCV002467956 RCV002530011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Asn1497Ser
CA7534658
NM_001160227.2:c.4490A>G