Canonical Allele Identifier: PA2827292905
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2008823
ClinVar RCV Id: RCV002828904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Pro1939Leu
CA384889653
NM_001330260.2:c.5816C>T