Allele Registry

Canonical Allele Identifier: PA2825844441

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000353970

RCV001549670

RCV002494949

RCV003380546

ClinVar Variation:

302646

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135820.1:p.Thr27Arg	CA6300188 NM_001142348.2:c.80C>G