Canonical Allele Identifier: PA2827292878
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1445246
ClinVar RCV Id: RCV001982820 RCV003355695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Thr1920Pro
CA384889193
NM_001330260.2:c.5758A>C