Allele Registry

Canonical Allele Identifier: PA2827069516

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000171052

RCV002515234

ClinVar Variation:

190872

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Val125Met	CA302176 NM_001321605.1:c.373G>A