Canonical Allele Identifier: PA2580370668
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1718528
ClinVar RCV Id: RCV002296665
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1751Val
CA384884943
NM_014191.4:c.5251A>G