Canonical Allele Identifier: PA2573256298
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1381300
ClinVar RCV Id: RCV001888657
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Tyr1883Cys
CA384888304
NM_014191.4:c.5648A>G