Allele Registry

Canonical Allele Identifier: PA2827763716

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059381

ClinVar Variation:

68509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Tyr413Asn	CA284877 NM_001353950.2:c.1237T>A