Allele Registry

Canonical Allele Identifier: PA2825844475

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000171769

RCV000306117

RCV000395598

RCV001082067

RCV001797657

RCV002354430

RCV003965229

ClinVar Variation:

191547

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Val69Met	CA236970 NM_001142348.2:c.205G>A