Canonical Allele Identifier: PA2741943065
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2810214
ClinVar RCV Id: RCV003754106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Pro1878Arg
CA384888230
NM_014191.4:c.5633C>G