Allele Registry

Canonical Allele Identifier: PA2827771671

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188988

ClinVar Variation:

206854

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Arg1637Leu	CA317561 NM_001353951.2:c.4910G>T