Canonical Allele Identifier: PA2826129486
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2642998
ClinVar RCV Id: RCV003391822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Leu219Val
CA385223871
NM_001177984.2:c.655C>G