Canonical Allele Identifier: PA2827769856
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 859315
ClinVar RCV Id: RCV001065394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu378Pro
CA349071148
NM_001353951.2:c.1133T>C