Allele Registry

Canonical Allele Identifier: PA2580108881

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV002636380

ClinVar Variation:

1936362

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg1463Cys	CA8708977 NM_000334.4:c.4387C>T