Canonical Allele Identifier: PA2825947527
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 466517
ClinVar RCV Id: RCV000528211 RCV003238770 RCV002438391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Glu958Asp
CA7535113
NM_001160227.2:c.2874A>C
CA392229563
NM_001160227.2:c.2874A>T