Allele Registry

Canonical Allele Identifier: PA2826009261

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000413776

RCV001328664

ClinVar Variation:

372865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Val421Met	CA16042397 NM_001165963.4:c.1261G>A