Canonical Allele Identifier: PA2827290956
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1723004
ClinVar RCV Id: RCV002306111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Tyr305Cys
CA385226819
NM_001330260.2:c.914A>G