Canonical Allele Identifier: PA2826129907
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1042516
ClinVar RCV Id: RCV001346485 RCV002431976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Lys718Arg
CA384879727
NM_001177984.2:c.2153A>G