Canonical Allele Identifier: PA2827771929
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 930321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Tyr1770His
CA349068092
NM_001353951.2:c.5308T>C