Canonical Allele Identifier: PA2580230045
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2203176
ClinVar RCV Id: RCV002664262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Met741Arg
CA349072190
NM_001353961.2:c.2222T>G