Canonical Allele Identifier: PA916036786
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12892
ClinVar RCV Id: RCV000013752 RCV000059508
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Val614Ala
CA256605
NM_001353961.2:c.1841T>C