Allele Registry

Canonical Allele Identifier: PA107833

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059552

RCV001569540

ClinVar Variation:

68672

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ile252Asn	CA285255 NM_001165963.4:c.755T>A