Allele Registry

Canonical Allele Identifier: PA2825352633

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000548321

ClinVar Variation:

470177

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Arg96Trp	CA9372001 NM_001037.5:c.286C>T