Allele Registry

Canonical Allele Identifier: PA1139741364

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001070909

ClinVar Variation:

863847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Pro934Arg	CA349068404 NM_001353961.2:c.2801C>G