Allele Registry

Canonical Allele Identifier: PA2826012502

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001035614

ClinVar Variation:

834846

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Thr847Arg	CA349061726 NM_001165964.3:c.2540C>G