Canonical Allele Identifier: PA2573256294
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1391051
ClinVar RCV Id: RCV001889702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ser1882Pro
CA384888285
NM_014191.4:c.5644T>C