Allele Registry

Canonical Allele Identifier: PA2829676065

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000489011

RCV001257670

ClinVar Variation:

426175

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Val1470Ile	CA349049242 NM_006920.6:c.4408G>A