Canonical Allele Identifier: PA2828361462
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1399569
ClinVar RCV Id: RCV001917752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Gly1701Ala
CA384884637
NM_001369788.1:c.5102G>C