Allele Registry

Canonical Allele Identifier: PA199798

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000171568

RCV000234662

RCV000490150

RCV002354426

ClinVar Variation:

191380

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Ser206Leu	CA199796 NM_174934.4:c.617C>T