Allele Registry

Canonical Allele Identifier: PA2826260318

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059435

ClinVar Variation:

68560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Thr1658Arg	CA284994 NM_001202435.3:c.4973C>G