Allele Registry

Canonical Allele Identifier: PA645407752

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000490238

ClinVar Variation:

426288

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Phe1619Ser	CA349037607 NM_021007.3:c.4856T>C