Allele Registry

Canonical Allele Identifier: PA2827782677

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000724139

RCV000795103

ClinVar Variation:

194616

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Asp1031Val	CA240690 NM_001353957.2:c.3092A>T