Allele Registry

Canonical Allele Identifier: PA645407671

Gene: SCN2A HGNC NCBI

ClinVar Allele:

365796

ClinVar RCV:

RCV000431611

RCV003233637

ClinVar Variation:

392633

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Trp923Arg	CA16603904 NM_021007.3:c.2767T>C CA349015396 NM_021007.3:c.2767T>A