Canonical Allele Identifier: PA2828361434
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1064808
ClinVar RCV Id: RCV001374961
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Met1654Thr
CA384883054
NM_001369788.1:c.4961T>C