Allele Registry

Canonical Allele Identifier: PA645449569

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000239745

RCV000523884

RCV000704631

RCV003992248

ClinVar Variation:

253297

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Arg1872Gln	CA10586302 NM_014191.4:c.5615G>A