Allele Registry

Canonical Allele Identifier: PA645406969

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000486566

ClinVar Variation:

421263

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Leu259Ile	CA16617262 NM_021007.3:c.775C>A