Allele Registry

Canonical Allele Identifier: PA2825354119

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000478420

ClinVar Variation:

421470

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Thr435Ile	CA16617263 NM_001040142.2:c.1304C>T