Canonical Allele Identifier: PA2826130776
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 420831
ClinVar RCV Id: RCV000481897 RCV001215479 RCV000762898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Met1828Thr
CA16619566
NM_001177984.2:c.5483T>C