Canonical Allele Identifier: PA916036870
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637
ClinVar RCV Id: RCV000059516 RCV003588571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gly772Glu
CA285180
NM_001353961.2:c.2315G>A