Allele Registry

Canonical Allele Identifier: PA916036919

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059435

ClinVar Variation:

68560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Thr844Arg	CA284994 NM_001353961.2:c.2531C>G