Allele Registry

Canonical Allele Identifier: PA093190

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000054537

RCV000485749

RCV000763041

RCV001059134

RCV002453365

RCV004542717

ClinVar Variation:

60767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Arg85His	CA144661 NM_001037.5:c.254G>A