Canonical Allele Identifier: PA2827291942
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1431533
ClinVar RCV Id: RCV001967556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ser1122Cys
CA6571582
NM_001330260.2:c.3364A>T