Allele Registry

Canonical Allele Identifier: PA1139724031

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001224613

ClinVar Variation:

952494

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Ile1479Leu	CA384909033 NM_014191.4:c.4435A>C