Allele Registry

Canonical Allele Identifier: PA2825844446

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000128817

ClinVar Variation:

140601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Ile32Leu	CA163448 NM_001142348.2:c.94A>C