Allele Registry

Canonical Allele Identifier: PA916055794

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000819241

ClinVar Variation:

661756

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Asp343Gly	CA349019879 NM_021007.3:c.1028A>G