Canonical Allele Identifier: PA2828361662
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013956
ClinVar RCV Id: RCV001312620
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Gly1923Arg
CA6571966
NM_001369788.1:c.5767G>A
CA384890300
NM_001369788.1:c.5767G>C