Canonical Allele Identifier: PA2827292864
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2957635
ClinVar RCV Id: RCV003811298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg1913Gln
CA384889029
NM_001330260.2:c.5738G>A