Allele Registry

Canonical Allele Identifier: PA234859

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000153892

RCV002516100

ClinVar Variation:

167641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Phe995Cys	CA234856 NM_001165963.4:c.2984T>G