Canonical Allele Identifier: PA2826130798
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2766850
ClinVar RCV Id: RCV003590448
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ser1841Phe
CA384888291
NM_001177984.2:c.5522C>T