Canonical Allele Identifier: PA2827781594
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Cys257Arg
CA303350
NM_001353957.2:c.769T>C