Allele Registry

Canonical Allele Identifier: PA2827771663

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180961

ClinVar Variation:

190005

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Arg1634Pro	CA303527 NM_001353951.2:c.4901G>C