Allele Registry

Canonical Allele Identifier: PA093332

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000006270

RCV002267603

ClinVar Variation:

5907

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Leu1433Arg	CA117844 NM_000334.4:c.4298T>G