Canonical Allele Identifier: PA2827778518
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2826806
ClinVar RCV Id: RCV003754372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Leu209Arg
CA349074317
NM_001353955.2:c.626T>G