Allele Registry

Canonical Allele Identifier: PA645407701

Gene: SCN2A HGNC NCBI

ClinVar Allele:

391627

ClinVar RCV:

RCV000469153

RCV001270400

RCV002510575

ClinVar Variation:

410982

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Arg1319Trp	CA1940198 NM_021007.3:c.3955C>T