Allele Registry

Canonical Allele Identifier: PA916036962

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059439

ClinVar Variation:

68564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met900Arg	CA285003 NM_001353961.2:c.2699T>G