Allele Registry

Canonical Allele Identifier: PA645415901

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000416448

ClinVar Variation:

375404

HGVS (amino-acid)	Matching Registered Transcripts
NP_950238.1:p.Asp103Val	CA16044237 NM_199037.5:c.308A>T