Canonical Allele Identifier: PA2826130822
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1064572
ClinVar RCV Id: RCV001374619 RCV001815543 RCV001865865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1866Trp
CA6571943
NM_001177984.2:c.5596C>T