Allele Registry

Canonical Allele Identifier: PA093161

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000006276

RCV000020262

RCV000206901

RCV001092728

ClinVar Variation:

5913

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg672Gly	CA253653 NM_000334.4:c.2014C>G