Canonical Allele Identifier: PA2825948157
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 406511
ClinVar RCV Id: RCV000458996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.His1757Tyr
CA16614609
NM_001160227.2:c.5269C>T