Canonical Allele Identifier: PA2826129950
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 834196
ClinVar RCV Id: RCV001034832 RCV003389858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Val787Ile
CA384880213
NM_001177984.2:c.2359G>A