Allele Registry

Canonical Allele Identifier: PA2826013367

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188949

RCV000766760

RCV001211105

ClinVar Variation:

206826

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Leu1421Phe	CA317455 NM_001165964.3:c.4261C>T