Allele Registry

Canonical Allele Identifier: PA645396364

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000274637

RCV004021498

ClinVar Variation:

302648

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Phe59Ser	CA6300283 NM_174934.4:c.176T>C