Allele Registry

Canonical Allele Identifier: PA2825359518

Gene: SCN2A HGNC NCBI

ClinVar Allele:

1368497

ClinVar RCV:

RCV001965466

ClinVar Variation:

1440047

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035233.1:p.Phe1213Cys	CA349026299 NM_001040143.2:c.3638T>G