Allele Registry

Canonical Allele Identifier: PA658668860

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000517575

ClinVar Variation:

448266

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Ser804Cys	CA400627209 NM_000334.4:c.2411C>G