Canonical Allele Identifier: PA2827771314
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2756858
ClinVar RCV Id: RCV003590134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ile1426Val
CA349049591
NM_001353951.2:c.4276A>G