Canonical Allele Identifier: PA2826129490
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 665356
ClinVar RCV Id: RCV000823620 RCV003236850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg223Ser
CA385223977
NM_001177984.2:c.669G>C
CA385223979
NM_001177984.2:c.669G>T