Allele Registry

Canonical Allele Identifier: PA3057399400

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV004954856

ClinVar Variation:

3438206

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Ile1566Phe	CA349036540 NM_021007.3:c.4696A>T