Allele Registry

Canonical Allele Identifier: PA2828473001

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001767965

ClinVar Variation:

1317399

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Ser1680Phe	CA349038055 NM_001371246.1:c.5039C>T