Allele Registry

Canonical Allele Identifier: PA2825356765

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001847356

RCV002319728

RCV002545228

ClinVar Variation:

1342682

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Ile1571Thr	CA349036596 NM_001040142.2:c.4712T>C