Allele Registry

Canonical Allele Identifier: PA093499

Gene: SCN8A HGNC NCBI

ClinVar Allele:

165903

ClinVar RCV:

RCV000144154

RCV000522954

RCV000636307

RCV000678845

RCV001266283

RCV003992195

ClinVar Variation:

156106

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Arg1617Gln	CA170757 NM_014191.4:c.4850G>A