Allele Registry

Canonical Allele Identifier: PA645404405

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000472521

ClinVar Variation:

408936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Leu1423Val	CA16610151 NM_001165963.4:c.4267C>G