Allele Registry

Canonical Allele Identifier: PA2827069253

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV001901765

ClinVar Variation:

1404685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Thr31Ala	CA405328331 NM_001321605.1:c.91A>G