Canonical Allele Identifier: PA2828360502
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 995250
ClinVar RCV Id: RCV001289207 RCV002537986 RCV004531064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Leu503Val
CA385228958
NM_001369788.1:c.1507C>G