Canonical Allele Identifier: PA2828733389
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1686225
ClinVar RCV Id: RCV002246738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Glu388Gly
CA346501865
NM_001377959.1:c.1163A>G