Canonical Allele Identifier: PA2826129499
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 870607
ClinVar RCV Id: RCV001090183 RCV003150822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Val233Leu
CA385224130
NM_001177984.2:c.697G>C
CA385224134
NM_001177984.2:c.697G>T