Allele Registry

Canonical Allele Identifier: PA2825844454

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000002563

ClinVar Variation:

2459

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Leu45Phe	CA252286 NM_001142348.2:c.133C>T