Allele Registry

Canonical Allele Identifier: PA2826260682

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000484175

RCV001057823

ClinVar Variation:

195945

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Pro1855Ser	CA242660 NM_001202435.3:c.5563C>T