Allele Registry

Canonical Allele Identifier: PA658809594

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636279

ClinVar Variation:

530420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ala1724Val	CA349068800 NM_001165963.4:c.5171C>T