Canonical Allele Identifier: PA2826258595
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1493044
ClinVar RCV Id: RCV001984069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Glu443Gln
CA349070494
NM_001202435.3:c.1327G>C