Canonical Allele Identifier: PA2826258700
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2715650
ClinVar RCV Id: RCV003590626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.His553Gln
CA349068232
NM_001202435.3:c.1659C>G
CA349068234
NM_001202435.3:c.1659C>A