Allele Registry

Canonical Allele Identifier: PA2827771927

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000489093

ClinVar Variation:

427080

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Met1769Val	CA349068113 NM_001353951.2:c.5305A>G