Allele Registry

Canonical Allele Identifier: PA303253

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180852

ClinVar Variation:

189900

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Trp738Leu	CA303250 NM_001165963.4:c.2213G>T