Canonical Allele Identifier: PA2826129537
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1325766
ClinVar RCV Id: RCV001785303 RCV003125907 RCV003992552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly269Arg
CA385226558
NM_001177984.2:c.805G>A
CA385226559
NM_001177984.2:c.805G>C