Allele Registry

Canonical Allele Identifier: PA916036970

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000554528

ClinVar Variation:

461279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ser909Pro	CA349068817 NM_001353961.2:c.2725T>C