Allele Registry

Canonical Allele Identifier: PA1139741405

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001195896

RCV001863098

ClinVar Variation:

930321

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Tyr967His	CA349068092 NM_001353961.2:c.2899T>C