Allele Registry

Canonical Allele Identifier: PA2826013697

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188988

ClinVar Variation:

206854

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Arg1620Leu	CA317561 NM_001165964.3:c.4859G>T