Allele Registry

Canonical Allele Identifier: PA2829675977

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000231750

ClinVar Variation:

238603

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Val1417Phe	CA10581821 NM_006920.6:c.4249G>T