Canonical Allele Identifier: PA2827787788
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1349279
ClinVar RCV Id: RCV002051017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Tyr399His
CA349071007
NM_001353960.2:c.1195T>C