Allele Registry

Canonical Allele Identifier: PA2827777780

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059439

ClinVar Variation:

68564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340883.1:p.Met1702Arg	CA285003 NM_001353954.2:c.5105T>G