Canonical Allele Identifier: PA2825947756
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 862012
ClinVar RCV Id: RCV001068643 RCV004546598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala1237Val
CA7534861
NM_001160227.2:c.3710C>T