Canonical Allele Identifier: PA2741943072
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2766850
ClinVar RCV Id: RCV003590448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ser1882Phe
CA384888291
NM_014191.4:c.5645C>T