Canonical Allele Identifier: PA2828124970
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2229241
ClinVar RCV Id: RCV002692595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Val108Gly
CA346602283
NM_001363875.2:c.323T>G