Canonical Allele Identifier: PA916036649
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 516847
ClinVar RCV Id: RCV000600699 RCV001401866 RCV002066773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg399Gln
CA1942908
NM_001353961.2:c.1196G>A