Allele Registry

Canonical Allele Identifier: PA279125

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000201212

RCV001209122

ClinVar Variation:

217263

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg1457His	CA279124 NM_000334.4:c.4370G>A