Canonical Allele Identifier: PA2573211266
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1399415
ClinVar RCV Id: RCV001922799 RCV003987932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Val211Gly
CA385224433
NM_001369788.1:c.632T>G