Allele Registry

Canonical Allele Identifier: PA302191

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000171059

RCV002517646

RCV004020041

ClinVar Variation:

190879

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Asp25Asn	CA302190 NM_001037.5:c.73G>A