Allele Registry

Canonical Allele Identifier: PA915978583

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000002563

ClinVar Variation:

2459

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135821.1:p.Leu69Phe	CA252286 NM_001142349.2:c.205C>T