Allele Registry

Canonical Allele Identifier: PA2825356876

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000414308

ClinVar Variation:

372556

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Ser1621Pro	CA16042357 NM_001040142.2:c.4861T>C