Allele Registry

Canonical Allele Identifier: PA2827774288

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000231750

ClinVar Variation:

238603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Val1417Phe	CA10581821 NM_001353952.2:c.4249G>T