Allele Registry

Canonical Allele Identifier: PA2827069501

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000054538

RCV000171064

RCV000234993

RCV000620098

RCV000766769

RCV001853079

RCV002477176

ClinVar Variation:

60768

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Asp120Asn	CA144662 NM_001321605.1:c.358G>A