Canonical Allele Identifier: PA2827770879
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1969094
ClinVar RCV Id: RCV002755344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Pro1166del
CA2580064350
NM_001353951.2:c.3496_3498del