Canonical Allele Identifier: PA2826129969
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1325768
ClinVar RCV Id: RCV001785305 RCV003992554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly822Arg
CA384884105
NM_001177984.2:c.2464G>A
CA384884108
NM_001177984.2:c.2464G>C