Allele Registry

Canonical Allele Identifier: PA2827761532

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000194223

RCV001192960

ClinVar Variation:

212119

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Asn1768Ser	CA208252 NM_001353949.2:c.5303A>G