Allele Registry

Canonical Allele Identifier: PA105512

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000002563

ClinVar Variation:

2459

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Leu179Phe	CA252286 NM_174934.4:c.535C>T