Allele Registry

Canonical Allele Identifier: PA2827069326

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV001340705

ClinVar Variation:

1037537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Glu54Lys	CA9371997 NM_001321605.1:c.160G>A