Allele Registry

Canonical Allele Identifier: PA2827789918

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000484175

RCV001057823

ClinVar Variation:

195945

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Pro1826Ser	CA242660 NM_001353960.2:c.5476C>T