Canonical Allele Identifier: PA2825948565
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 316078
ClinVar RCV Id: RCV000459952 RCV001541266 RCV002365370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Arg2180Trp
CA7533963
NM_001160227.2:c.6538C>T