Allele Registry

Canonical Allele Identifier: PA2825352690

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000417192

ClinVar Variation:

375687

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Ile106Phe	CA405328764 NM_001037.5:c.316A>T