Canonical Allele Identifier: PA2827291527
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2848664
ClinVar RCV Id: RCV003754683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.His775Tyr
CA384880128
NM_001330260.2:c.2323C>T