Allele Registry

Canonical Allele Identifier: PA2826259573

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180987

RCV001035456

ClinVar Variation:

190031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Glu1221Gln	CA303606 NM_001202435.3:c.3661G>C