Allele Registry

Canonical Allele Identifier: PA645406962

Gene: SCN2A HGNC NCBI

ClinVar Allele:

359401

ClinVar RCV:

RCV000413157

RCV001848732

ClinVar Variation:

372557

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Ser214Pro	CA16042425 NM_021007.3:c.640T>C