Allele Registry

Canonical Allele Identifier: PA2825352581

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV001340705

ClinVar Variation:

1037537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Glu87Lys	CA9371997 NM_001037.5:c.259G>A