Allele Registry

Canonical Allele Identifier: PA658668840

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000558352

RCV001785663

ClinVar Variation:

477400

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Gly526Arg	CA8709806 NM_000334.4:c.1576G>A CA400634465 NM_000334.4:c.1576G>C