Allele Registry

Canonical Allele Identifier: PA2573276154

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001965466

ClinVar Variation:

1440047

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Phe1213Cys	CA349026299 NM_021007.3:c.3638T>G