Allele Registry

Canonical Allele Identifier: PA1139724446

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001206283

ClinVar Variation:

937302

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Arg1820Gln	CA236327645 NM_014191.4:c.5459G>A