Allele Registry

Canonical Allele Identifier: PA2827771297

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000231750

ClinVar Variation:

238603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Val1417Phe	CA10581821 NM_001353951.2:c.4249G>T