Allele Registry

Canonical Allele Identifier: PA2741942945

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV003752670

ClinVar Variation:

2864798

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Lys1632Asn	CA384880462 NM_014191.4:c.4896A>C CA384880463 NM_014191.4:c.4896A>T