Allele Registry

Canonical Allele Identifier: PA2827069318

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000054537

RCV000485749

RCV000763041

RCV001059134

RCV002453365

RCV004542717

ClinVar Variation:

60767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Arg52His	CA144661 NM_001321605.1:c.155G>A