Allele Registry

Canonical Allele Identifier: PA2827781858

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180833

ClinVar Variation:

189880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Met400Lys	CA303192 NM_001353957.2:c.1199T>A