Allele Registry

Canonical Allele Identifier: PA2826260554

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000194223

RCV001192960

ClinVar Variation:

212119

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Asn1779Ser	CA208252 NM_001202435.3:c.5336A>G