Allele Registry

Canonical Allele Identifier: PA234858

Gene: SCN1A HGNC NCBI

ClinVar Allele:

176938

ClinVar RCV:

RCV000153892

RCV002516100

ClinVar Variation:

167641

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe984Cys	CA234856 NM_006920.6:c.2951T>G