Allele Registry

Canonical Allele Identifier: PA916037003

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000176636

RCV001852177

ClinVar Variation:

195946

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Asn965Asp	CA242664 NM_001353961.2:c.2893A>G