Canonical Allele Identifier: PA2826130868
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013956
ClinVar RCV Id: RCV001312620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly1923Arg
CA6571966
NM_001177984.2:c.5767G>A
CA384890300
NM_001177984.2:c.5767G>C