Canonical Allele Identifier: PA2828124853
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1405016
ClinVar RCV Id: RCV001903520 RCV002473320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ser13Thr
CA1600460
NM_001363875.2:c.37T>A