Canonical Allele Identifier: PA2827786879
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2710218
ClinVar RCV Id: RCV003589968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Glu1782Asp
CA349067612
NM_001353958.2:c.5346G>T
CA349067613
NM_001353958.2:c.5346G>C