Canonical Allele Identifier: PA2828360893
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1023685
ClinVar RCV Id: RCV001323769
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Asp991Asn
CA236318491
NM_001369788.1:c.2971G>A