Canonical Allele Identifier: PA2828120787
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 378639
ClinVar RCV Id: RCV000424051 RCV002521540 RCV002524804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Gln82Glu
CA8243475
NM_001363850.1:c.244C>G