Allele Registry

Canonical Allele Identifier: PA093462

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000006277

RCV000235023

ClinVar Variation:

5914

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Val1442Glu	CA117848 NM_000334.4:c.4325T>A