Canonical Allele Identifier: PA2741866860
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2710218
ClinVar RCV Id: RCV003589968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Glu996Asp
CA349067612
NM_001353961.2:c.2988G>T
CA349067613
NM_001353961.2:c.2988G>C