Canonical Allele Identifier: PA2828361498
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 3067149
ClinVar RCV Id: RCV003992838
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Thr1746Pro
CA384885532
NM_001369788.1:c.5236A>C