Allele Registry

Canonical Allele Identifier: PA2826259216

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180835

ClinVar Variation:

189882

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Arg946Pro	CA303197 NM_001202435.3:c.2837G>C