Allele Registry

Canonical Allele Identifier: PA093419

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000006261

RCV000489309

RCV001799586

RCV003505081

ClinVar Variation:

5901

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Ser804Phe	CA117838 NM_000334.4:c.2411C>T