Allele Registry

Canonical Allele Identifier: PA2828475752

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000013736

RCV001851831

RCV002319420

ClinVar Variation:

12876

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Leu1330Phe	CA122768 NM_001371247.1:c.3988C>T