Canonical Allele Identifier: PA2828360711
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1011721
ClinVar RCV Id: RCV001309560
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Thr729Pro
CA384879805
NM_001369788.1:c.2185A>C