Allele Registry

Canonical Allele Identifier: PA2826260622

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003129159

ClinVar Variation:

2430626

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Lys1814Asn	CA349067542 NM_001202435.3:c.5442G>T CA349067544 NM_001202435.3:c.5442G>C