Allele Registry

Canonical Allele Identifier: PA2741974388

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV003797141

ClinVar Variation:

2938319

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Cys1181Phe	CA1940133 NM_021007.3:c.3542G>T