Canonical Allele Identifier: PA2828121015
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215211
ClinVar RCV Id: RCV000713479 RCV000804015 RCV003488456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Gly423Ser
CA324322
NM_001363850.1:c.1267G>A