Canonical Allele Identifier: PA2827765149
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68523
ClinVar RCV Id: RCV000059395 RCV000378734 RCV000543457 RCV001004709 RCV001264404 RCV002433566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Arg935His
CA284910
NM_001353950.2:c.2804G>A