Canonical Allele Identifier: PA645449052
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 236207
ClinVar RCV Id: RCV000225160 RCV001232816
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Leu267Ser
CA10581564
NM_014191.4:c.800T>C