Allele Registry

Canonical Allele Identifier: PA2828473960

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000022770

RCV002319427

ClinVar Variation:

29889

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358176.1:p.Met252Val	CA128713 NM_001371247.1:c.754A>G