Canonical Allele Identifier: PA2828360897
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1016014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Asn995Lys
CA384892045
NM_001369788.1:c.2985C>A
CA384892046
NM_001369788.1:c.2985C>G