Allele Registry

Canonical Allele Identifier: PA645453757

Gene: SCN4A HGNC NCBI

ClinVar Allele:

329392

ClinVar RCV:

RCV000290622

RCV000345319

RCV000384970

RCV000393903

RCV000813822

ClinVar Variation:

324508

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Gly1762Arg	CA8708790 NM_000334.4:c.5284G>A CA400613025 NM_000334.4:c.5284G>C