Canonical Allele Identifier: PA2828360716
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 3061364
ClinVar RCV Id: RCV004542679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ile732Met
CA384879828
NM_001369788.1:c.2196C>G