Allele Registry

Canonical Allele Identifier: PA2826013896

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001070909

ClinVar Variation:

863847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Pro1720Arg	CA349068404 NM_001165964.3:c.5159C>G