Allele Registry

Canonical Allele Identifier: PA2828470521

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000416990

RCV003985327

ClinVar Variation:

375507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Trp191Gly	CA16044305 NM_001371246.1:c.571T>G