Allele Registry

Canonical Allele Identifier: PA2825361256

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV001797221

RCV004040854

ClinVar Variation:

1328589

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035241.1:p.Ala130Glu	CA229983987 NM_001040151.2:c.389C>A