Allele Registry

Canonical Allele Identifier: PA2827786193

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000231750

ClinVar Variation:

238603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Val1400Phe	CA10581821 NM_001353958.2:c.4198G>T