Allele Registry

Canonical Allele Identifier: PA916061743

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000500892

RCV000620273

RCV001127219

RCV002223804

RCV003448275

ClinVar Variation:

190859

HGVS (amino-acid)	Matching Registered Transcripts
NP_950238.1:p.Arg85Cys	CA302153 NM_199037.5:c.253C>T