Canonical Allele Identifier: PA2828360357
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1723004
ClinVar RCV Id: RCV002306111
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Tyr305Cys
CA385226819
NM_001369788.1:c.914A>G