Allele Registry

Canonical Allele Identifier: PA2827767810

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059439

ClinVar Variation:

68564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Met1703Arg	CA285003 NM_001353950.2:c.5108T>G