Allele Registry

Canonical Allele Identifier: PA2573205785

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002021598

ClinVar Variation:

1518250

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ile968Leu	CA349068079 NM_001353961.2:c.2902A>C