Allele Registry

Canonical Allele Identifier: PA2828470692

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000422511

ClinVar Variation:

391613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Asp343Val	CA16603896 NM_001371246.1:c.1028A>T