Canonical Allele Identifier: PA2826130137
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1878660
ClinVar RCV Id: RCV002510751 RCV003776050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asp1035Asn
CA6571545
NM_001177984.2:c.3103G>A