Allele Registry

Canonical Allele Identifier: PA915978620

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000171568

RCV000234662

RCV000490150

RCV002354426

ClinVar Variation:

191380

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135821.1:p.Ser96Leu	CA199796 NM_001142349.2:c.287C>T