Allele Registry

Canonical Allele Identifier: PA645402960

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000413776

RCV001328664

ClinVar Variation:

372865

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Val421Met	CA16042397 NM_006920.6:c.1261G>A