Canonical Allele Identifier: PA2741943077
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2961616
ClinVar RCV Id: RCV003822262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly1908Arg
CA6571945
NM_014191.4:c.5722G>A
CA384888909
NM_014191.4:c.5722G>C