Canonical Allele Identifier: PA2827768194
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2710218
ClinVar RCV Id: RCV003589968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Glu1799Asp
CA349067612
NM_001353950.2:c.5397G>T
CA349067613
NM_001353950.2:c.5397G>C