Canonical Allele Identifier: PA325313
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215219
ClinVar RCV Id: RCV000227318 RCV000766856 RCV001847890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Ala759Thr
CA325312
NM_003119.4:c.2275G>A