Canonical Allele Identifier: PA645449143
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 309354
ClinVar RCV Id: RCV000312849
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Tyr811Cys
CA10633090
NM_014191.4:c.2432A>G