Allele Registry

Canonical Allele Identifier: PA2827770472

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001035614

ClinVar Variation:

834846

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Thr864Arg	CA349061726 NM_001353951.2:c.2591C>G