Allele Registry

Canonical Allele Identifier: PA303169

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180825

RCV003326125

ClinVar Variation:

189872

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Pro358Ser	CA303166 NM_006920.6:c.1072C>T