Allele Registry

Canonical Allele Identifier: PA2827786301

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000489011

RCV001257670

ClinVar Variation:

426175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Val1453Ile	CA349049242 NM_001353958.2:c.4357G>A