Allele Registry

Canonical Allele Identifier: PA2573093631

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV001797221

RCV004040854

ClinVar Variation:

1328589

HGVS (amino-acid)	Matching Registered Transcripts
NP_060870.1:p.Ala130Glu	CA229983987 NM_018400.3:c.389C>A