Canonical Allele Identifier: PA2827292840
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 546708
ClinVar RCV Id: RCV000658650 RCV001215294
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg1891His
CA384888435
NM_001330260.2:c.5672G>A