Allele Registry

Canonical Allele Identifier: PA2828472939

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001311936

ClinVar Variation:

1013421

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Leu1650Phe	CA349037845 NM_001371246.1:c.4948C>T