Allele Registry

Canonical Allele Identifier: PA2829965957

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV002272935

ClinVar Variation:

1699078

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Phe1527_Asp1534del	CA2573130278 NM_021007.3:c.4579_4602del