Canonical Allele Identifier: PA2827290832
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2036663
ClinVar RCV Id: RCV002882014
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Leu213Pro
CA385224481
NM_001330260.2:c.638T>C