Canonical Allele Identifier: PA916011977
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 807679
ClinVar RCV Id: RCV000995865
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Leu849His
CA384886415
NM_014191.4:c.2546T>A