Canonical Allele Identifier: PA2828361648
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1936334
ClinVar RCV Id: RCV002642539
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Pro1904Leu
CA6571959
NM_001369788.1:c.5711C>T