Allele Registry

Canonical Allele Identifier: PA2826260625

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001065356

ClinVar Variation:

859283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Phe1815Ser	CA349067529 NM_001202435.3:c.5444T>C