Allele Registry

Canonical Allele Identifier: PA2827775923

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180872

ClinVar Variation:

189920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340883.1:p.Val422Ala	CA303306 NM_001353954.2:c.1265T>C