Allele Registry

Canonical Allele Identifier: PA2827753560

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000231750

ClinVar Variation:

238603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Val1428Phe	CA10581821 NM_001353948.2:c.4282G>T