Canonical Allele Identifier: PA2827773921
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801478
ClinVar RCV Id: RCV002463567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Glu1205Gln
CA349056032
NM_001353952.2:c.3613G>C