Canonical Allele Identifier: PA266113
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68625
ClinVar RCV Id: RCV000059503 RCV000188936 RCV001786331 RCV001220193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu1298Phe
CA266111
NM_006920.6:c.3892C>T