Canonical Allele Identifier: PA2827758451
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Arg920Cys
CA273369
NM_001353949.2:c.2758C>T