Allele Registry

Canonical Allele Identifier: PA2827780781

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059441

ClinVar Variation:

68566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Thr1709Arg	CA285009 NM_001353955.2:c.5126C>G