Canonical Allele Identifier: PA2828361126
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1691849
ClinVar RCV Id: RCV002255237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Gly1281Arg
CA384904441
NM_001369788.1:c.3841G>C