Allele Registry

Canonical Allele Identifier: PA2825844442

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000128816

ClinVar Variation:

140600

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Val28Gly	CA163446 NM_001142348.2:c.83T>G