Allele Registry

Canonical Allele Identifier: PA2827790202

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001035614

ClinVar Variation:

834846

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Thr61Arg	CA349061726 NM_001353961.2:c.182C>G