Allele Registry

Canonical Allele Identifier: PA658660960

Gene: SCN2A HGNC NCBI

ClinVar Allele:

442983

ClinVar RCV:

RCV000688798

RCV000720902

RCV001004701

RCV001783018

RCV001848910

RCV003147500

ClinVar Variation:

449147

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Ala202Val	CA349016810 NM_021007.3:c.605C>T