Canonical Allele Identifier: PA2828360924
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1995109
ClinVar RCV Id: RCV002791638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Asp1029Val
CA384892360
NM_001369788.1:c.3086A>T