Canonical Allele Identifier: PA2827789700
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 834858
ClinVar RCV Id: RCV001035628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asp1698Tyr
CA349068756
NM_001353960.2:c.5092G>T