Allele Registry

Canonical Allele Identifier: PA1139725950

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001206716

RCV002282481

ClinVar Variation:

937654

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Trp1565Arg	CA349036523 NM_021007.3:c.4693T>C CA349036526 NM_021007.3:c.4693T>A