Allele Registry

Canonical Allele Identifier: PA093152

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000206949

RCV002307367

RCV003482229

ClinVar Variation:

21151

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg672Cys	CA341668 NM_000334.4:c.2014C>T