Allele Registry

Canonical Allele Identifier: PA2827292722

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001206283

ClinVar Variation:

937302

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Arg1820Gln	CA236327645 NM_001330260.2:c.5459G>A