Canonical Allele Identifier: PA2828361603
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 546708
ClinVar RCV Id: RCV000658650 RCV001215294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1850His
CA384888435
NM_001369788.1:c.5549G>A