Allele Registry

Canonical Allele Identifier: PA916055776

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000022770

RCV002319427

ClinVar Variation:

29889

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Met252Val	CA128713 NM_021007.3:c.754A>G