Allele Registry

Canonical Allele Identifier: PA1139740458

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001065356

ClinVar Variation:

859283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Phe1815Ser	CA349067529 NM_001353948.2:c.5444T>C