Canonical Allele Identifier: PA2827292868
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2097452
ClinVar RCV Id: RCV003018820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Gly1914Asp
CA384889047
NM_001330260.2:c.5741G>A