Allele Registry

Canonical Allele Identifier: PA2825352488

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV001901765

ClinVar Variation:

1404685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Thr64Ala	CA405328331 NM_001037.5:c.190A>G