Canonical Allele Identifier: PA2573256319
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1389834
ClinVar RCV Id: RCV001898094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Gly1914Cys
CA384889039
NM_014191.4:c.5740G>T