Allele Registry

Canonical Allele Identifier: PA093219

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000009837

RCV003332078

RCV003988820

ClinVar Variation:

9255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Glu87Gln	CA120244 NM_001037.5:c.259G>C