Allele Registry

Canonical Allele Identifier: PA645396377

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000482623

RCV000618216

RCV001451522

ClinVar Variation:

420671

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Leu181Pro	CA6300170 NM_174934.4:c.542T>C