Canonical Allele Identifier: PA2827765179
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68605
ClinVar RCV Id: RCV000059482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Trp941Gly
CA285099
NM_001353950.2:c.2821T>G