Allele Registry

Canonical Allele Identifier: PA1139742017

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001261989

RCV001526607

ClinVar Variation:

982411

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Val261Leu	CA349018067 NM_021007.3:c.781G>C CA349018069 NM_021007.3:c.781G>T