Canonical Allele Identifier: PA2826130418
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 156107
ClinVar RCV Id: RCV000144155
ClinVar Variation Id: 2907429
ClinVar RCV Id: RCV003753672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asn1425Lys
CA170758
NM_001177984.2:c.4275C>A
CA384908571
NM_001177984.2:c.4275C>G