Allele Registry

Canonical Allele Identifier: PA658668869

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000538078

RCV001267294

RCV001335257

ClinVar Variation:

477408

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Asp932Asn	CA8709499 NM_000334.4:c.2794G>A