Allele Registry

Canonical Allele Identifier: PA105502

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000128817

ClinVar Variation:

140601

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Ile166Leu	CA163448 NM_174934.4:c.496A>C