Canonical Allele Identifier: PA2826130835
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_001171455.1:p.Thr1879Pro
CA384889193
NM_001177984.2:c.5635A>C