Canonical Allele Identifier: PA2827767536
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Arg1637His
CA256584
NM_001353950.2:c.4910G>A