Allele Registry

Canonical Allele Identifier: PA915978535

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000994731

RCV001227229

RCV002362871

ClinVar Variation:

190895

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Thr77Arg	CA302222 NM_001142348.2:c.230C>G