Allele Registry

Canonical Allele Identifier: PA915978610

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000171769

RCV000306117

RCV000395598

RCV001082067

RCV001797657

RCV002354430

RCV003965229

ClinVar Variation:

191547

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135821.1:p.Val93Met	CA236970 NM_001142349.2:c.277G>A