Canonical Allele Identifier: PA916047891
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 702258
ClinVar RCV Id: RCV001467506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Leu228Trp
CA385224812
NM_001369788.1:c.683T>G