Allele Registry

Canonical Allele Identifier: PA2827770274

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180852

ClinVar Variation:

189900

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Trp727Leu	CA303250 NM_001353951.2:c.2180G>T