Allele Registry

Canonical Allele Identifier: PA916037002

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000194223

RCV001192960

ClinVar Variation:

212119

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Asn965Ser	CA208252 NM_001353961.2:c.2894A>G