Allele Registry

Canonical Allele Identifier: PA303321

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180875

ClinVar Variation:

189923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ser1516Trp	CA303318 NM_001165963.4:c.4547C>G