Allele Registry

Canonical Allele Identifier: PA645407763

Gene: SCN2A HGNC NCBI

ClinVar Allele:

405356

ClinVar RCV:

RCV000480069

ClinVar Variation:

420819

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Met1655Thr	CA16617271 NM_021007.3:c.4964T>C