Canonical Allele Identifier: PA2828120711
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215198
ClinVar RCV Id: RCV000817246 RCV001847886 RCV001722098 RCV002515437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Ala2Thr
CA321845
NM_001363850.1:c.4G>A