Canonical Allele Identifier: PA2827783828
Gene: SCN1A HGNC NCBI
ClinVar RCV:
RCV000059442
ClinVar Variation:
68567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Gly1734Glu
CA285012
NM_001353957.2:c.5201G>A