Allele Registry

Canonical Allele Identifier: PA658809656

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636288

ClinVar Variation:

530427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Asp1866Gly	CA16602232 NM_001165963.4:c.5597A>G