Allele Registry

Canonical Allele Identifier: PA645404427

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000231750

ClinVar Variation:

238603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Val1428Phe	CA10581821 NM_001165963.4:c.4282G>T