Allele Registry

Canonical Allele Identifier: PA2827789156

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000472521

ClinVar Variation:

408936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Leu1394Val	CA16610151 NM_001353960.2:c.4180C>G