Allele Registry

Canonical Allele Identifier: PA302177

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000171052

RCV002515234

ClinVar Variation:

190872

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Val158Met	CA302176 NM_001037.5:c.472G>A