Allele Registry

Canonical Allele Identifier: PA096192

Gene: SCN2B HGNC NCBI

ClinVar RCV:

RCV000054539

RCV000483016

RCV002426610

ClinVar Variation:

60769

HGVS (amino-acid)	Matching Registered Transcripts
NP_004579.1:p.Arg28Trp	CA214436 NM_004588.5:c.82C>T