Allele Registry

Canonical Allele Identifier: PA916036406

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000022765

ClinVar Variation:

29884

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Arg862Gly	CA281752 NM_001353948.2:c.2584C>G