Canonical Allele Identifier: PA2826130861
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1317485
ClinVar RCV Id: RCV001768051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Thr1910Ser
CA384889926
NM_001177984.2:c.5728A>T
CA384889934
NM_001177984.2:c.5729C>G