Allele Registry

Canonical Allele Identifier: PA2825361238

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV000171068

RCV000185522

RCV000234992

RCV000621217

RCV000852659

RCV001087315

RCV003937532

ClinVar Variation:

190886

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035241.1:p.Val110Ile	CA235707 NM_001040151.2:c.328G>A