Canonical Allele Identifier: PA2825946761
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 413998
ClinVar RCV Id: RCV000457651 RCV001848827 RCV002253455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Ala59Val
CA7535932
NM_001160227.2:c.176C>T