Canonical Allele Identifier: PA2828125176
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 660105
ClinVar RCV Id: RCV000817235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Pro351Leu
CA346501303
NM_001363875.2:c.1052C>T