Allele Registry

Canonical Allele Identifier: PA915978561

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000128817

ClinVar Variation:

140601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135821.1:p.Ile56Leu	CA163448 NM_001142349.2:c.166A>C