Canonical Allele Identifier: PA2827788877
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2627518
ClinVar RCV Id: RCV003388781
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Phe1230Tyr
CA349054402
NM_001353960.2:c.3689T>A