Canonical Allele Identifier: PA2827772776
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Cys345Arg
CA303376
NM_001353952.2:c.1033T>C