Canonical Allele Identifier: PA2827291810
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1018267
ClinVar RCV Id: RCV001317542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg1026His
CA6571541
NM_001330260.2:c.3077G>A