Allele Registry

Canonical Allele Identifier: PA235715

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000171074

RCV000619132

RCV001078793

ClinVar Variation:

190891

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.His65Leu	CA235713 NM_174934.4:c.194A>T