Allele Registry

Canonical Allele Identifier: PA214235

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000454426

RCV000996832

RCV001372438

RCV001841546

ClinVar Variation:

36757

HGVS (amino-acid)	Matching Registered Transcripts
NP_950238.1:p.Val251Ile	CA214234 NM_199037.5:c.751G>A