Allele Registry

Canonical Allele Identifier: PA2825844428

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000171073

RCV000185523

RCV000619368

RCV001079013

RCV003937533

ClinVar Variation:

190890

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Gly8Ser	CA235710 NM_001142348.2:c.22G>A