Allele Registry

Canonical Allele Identifier: PA2828476321

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000013737

RCV000255820

RCV002319421

RCV002513022

ClinVar Variation:

12877

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Leu1563Val	CA122769 NM_001371247.1:c.4687C>G