Canonical Allele Identifier: PA2826130795
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1040115
ClinVar RCV Id: RCV001343699 RCV002508803
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Lys1839Glu
CA384888255
NM_001177984.2:c.5515A>G