Canonical Allele Identifier: PA2827779038
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2715650
ClinVar RCV Id: RCV003590626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.His552Gln
CA349068232
NM_001353955.2:c.1656C>G
CA349068234
NM_001353955.2:c.1656C>A