Allele Registry

Canonical Allele Identifier: PA645402864

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000258942

ClinVar Variation:

279592

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Ala342Glu	CA10602709 NM_006920.6:c.1025C>A