Allele Registry

Canonical Allele Identifier: PA915978585

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000482623

RCV000618216

RCV001451522

ClinVar Variation:

420671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135821.1:p.Leu71Pro	CA6300170 NM_001142349.2:c.212T>C