Allele Registry

Canonical Allele Identifier: PA2827757180

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059382

ClinVar Variation:

68510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Val422Glu	CA145232 NM_001353949.2:c.1265T>A