Canonical Allele Identifier: PA2827769645
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Cys257Arg
CA303350
NM_001353951.2:c.769T>C