Canonical Allele Identifier: PA2828119269
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448450
ClinVar RCV Id: RCV000517986 RCV000700492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Met576Arg
CA346505502
NM_001363823.2:c.1727T>G