Allele Registry

Canonical Allele Identifier: PA2827786949

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000484175

RCV001057823

ClinVar Variation:

195945

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Pro1827Ser	CA242660 NM_001353958.2:c.5479C>T