Allele Registry

Canonical Allele Identifier: PA645396373

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000353970

RCV001549670

RCV002494949

RCV003380546

ClinVar Variation:

302646

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Thr161Arg	CA6300188 NM_174934.4:c.482C>G