Canonical Allele Identifier: PA2827770618
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Cys948Arg
CA285105
NM_001353951.2:c.2842T>C