Allele Registry

Canonical Allele Identifier: PA093279

Gene: SCN4A HGNC NCBI

ClinVar Allele:

20954

ClinVar RCV:

RCV000006278

ClinVar Variation:

5915

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Gly1456Glu	CA117849 NM_000334.4:c.4367G>A